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- W2050476259 abstract "A multistep synthesis of a protected aza-C-disaccharide derivative with a pyrrolidine ring as the azasugar component is described. The key step is a stereoselective cycloaddition reaction of a chiral nitrone derived from D-ribose and a sugar alkene derived from D-galactose. An intramolecular N-alkylation followed by a reductive cleavage of the isoxazolidine N–O bond, in one pot, gave the final product." @default.
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- W2050476259 date "2004-05-01" @default.
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- W2050476259 title "Synthesis of a branched chain aza-C-disaccharide via the cycloaddition of a chiral nitrone to an alkene, both sugar derivatives" @default.
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- W2050476259 doi "https://doi.org/10.1016/j.tetlet.2004.04.031" @default.
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